• CSA Z11137-2 : 2007 : R2012

    Superseded A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

    STERILIZATION OF HEALTH CARE PRODUCTS - RADIATION - PART 2: ESTABLISHING THE STERILIZATION DOSE

    Available format(s):  Hardcopy, PDF

    Superseded date:  01-07-2016

    Language(s):  English

    Published date:  01-01-2012

    Publisher:  Canadian Standards Association

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    Table of Contents - (Show below) - (Hide below)

    Foreword
    Introduction
    1 Scope
    2 Normative references
    3 Abbreviations, terms and definitions
       3.1 Abbreviations
       3.2 Terms
    4 Definition and maintenance of product families for
       dose setting, dose substantiation and sterilization
       dose auditing
       4.1 General
       4.2 Defining product families
       4.3 Designation of product to represent a product
            family for performance of a verification dose
            experiment or sterilization dose audit
       4.4 Maintaining product families
       4.5 Effect of failure of establishment of sterilization
            dose or of a sterilization dose audit on a product
            family
    5 Selection and testing of product for establishing and
       verifying the sterilization dose
       5.1 Nature of product
       5.2 Sample item portion (SIP)
       5.3 Manner of sampling
       5.4 Microbiological testing
       5.5 Irradiation
    6 Methods of dose establishment
    7 Method 1: dose setting using bioburden information
       7.1 Rationale
       7.2 Procedure for Method 1 for product with an average
            bioburden W 1,0 for multiple production batch
       7.3 Procedure for Method 1 for product with an average
            bioburden W 1,0 for a single production batch
       7.4 Procedure for Method 1 for product with an average
            bioburden in the range 0,1 to 0,9 for multiple or
            single production batches
    8 Method 2: Dose setting using fraction positive information
       from incremental dosing to determine an extrapolation
       factor
       8.1 Rationale
       8.2 Procedure for Method 2A
       8.3 Procedure for Method 2B
    9 Method VD[max] - Substantiation of 25 kGy or 15 kGy
       as the sterilization dose
       9.1 Rationale
       9.2 Procedure for Method VD[max][25] for multiple
            production batches
       9.3 Procedure for Method VD[max][25] for a single
            production batch
       9.4 Procedure for Method VD[max][15] for multiple
            production batches
       9.5 Procedure for Method VD[max][15] for a single
            production batch
    10 Auditing sterilization dose
       10.1 Purpose and
       10.2 Procedure for auditing a sterilization dose
            established using Method 1 or Method 2
       10.3 Procedure for auditing a sterilization dose
            substantiated using VD[max]
    11 Worked examples
       11.1 Worked examples for Method 1
       11.2 Worked examples for Method 2
       11.3 Worked examples for Method VD[max]
       11.4 Worked example of a sterilization dose audit
            for a dose established using Method 1, the
            findings from which necessitated augmentation
            of the sterilization dose
       11.5 Worked example of a sterilization dose audit
            for a dose established using Method 2A, the
            findings from which necessitated augmentation
            of the sterilization dose
       11.6 Worked example of a sterilization dose audit
            for a sterilization dose substantiated using
            Method VD[max][25]
    Bibliography

    Abstract - (Show below) - (Hide below)

    Describes methods of determining the minimum dose needed to achieve a specified requirement for sterility and methods to substantiate the use of 25 kGy or 15 kGy as the sterilization dose to achieve a sterility assurance level, SAL, of 10-6.

    General Product Information - (Show below) - (Hide below)

    Development Note Supersedes CSA ISO 11137. (01/2009)
    Document Type Standard
    Product Note Reconfirmed EN
    Publisher Canadian Standards Association
    Status Superseded
    Superseded By
    Supersedes

    Standards Referencing This Book - (Show below) - (Hide below)

    ISO 11137-1:2006 Sterilization of health care products Radiation Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices
    ISO 11737-2:2009 Sterilization of medical devices Microbiological methods Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process
    ISO 11737-1:2006 Sterilization of medical devices Microbiological methods Part 1: Determination of a population of microorganisms on products
    ISO 13485:2016 Medical devices Quality management systems Requirements for regulatory purposes
    AAMI TIR27 : 1ED 2001 STERILIZATION OF HEALTH CARE PRODUCTS - RADIATION STERILIZATION - SUBSTANTIATION OF 25 KGY AS A STERILIZATION DOSE - METHOD VD MAX
    AAMI ST32 : 1991 GUIDELINE FOR GAMMA RADIATION STERILIZATION
    ISO/TS 11139:2006 Sterilization of health care products Vocabulary
    ISO 11137-3:2017 Sterilization of health care products — Radiation — Part 3: Guidance on dosimetric aspects of development, validation and routine control
    ISO 14971:2007 Medical devices Application of risk management to medical devices
    ISO 11137:1995 Sterilization of health care products Requirements for validation and routine control Radiation sterilization
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